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肱尺关节创伤性骨化性桥接肌炎:一例报告

Humeroulnar Bridging Myositis Ossificans Traumatica: A Case Report.

作者信息

Singh Naveen Kumar, Kumar Deepak, Jaiswar Rohit Devnarayan

机构信息

Department of Orthopaedics, MLN Medical College, Prayagraj, Uttar Pradesh, India.

出版信息

J Orthop Case Rep. 2025 Sep;15(9):43-46. doi: 10.13107/jocr.2025.v15.i09.6008.

DOI:10.13107/jocr.2025.v15.i09.6008
PMID:40936839
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12422683/
Abstract

INTRODUCTION

Myositis ossificans traumatica (MOT) of the elbow is a rare entity in children. It is a self-localized tumor-like lesion of the elbow causing ankylosis due to humeroulnar bridging. It is a complication arising due to a muscle contusion injury.

CASE REPORT

We report a case of an 8-year-old female who presented with a 2-year history of a fixed elbow and a palpable bony mass. The examination confirmed a confined bony mass on the anterior aspect and ankylosis of her left elbow. On confirmation of the diagnosis, an en bloc excision was performed. Follow-up every 2 weeks for the first 3 months, then once a month for the next 6 months, and finally once every 6 months for the next 4 years. The affected limb functioned well, with no sign of recurrence.

CONCLUSION

MOTs of the elbow in children are a rarity, and excision of the lesion without delay is an effective management strategy for a satisfactory outcome.

摘要

引言

儿童肘部创伤性骨化性肌炎(MOT)较为罕见。它是肘部一种自限性肿瘤样病变,因肱尺关节桥接导致关节强直。它是肌肉挫伤损伤引起的一种并发症。

病例报告

我们报告一例8岁女性,有2年肘部固定及可触及骨性肿块的病史。检查证实左肘前方有局限性骨性肿块及关节强直。确诊后,进行了整块切除。最初3个月每2周随访一次,接下来6个月每月随访一次,最后4年每6个月随访一次。患侧肢体功能良好,无复发迹象。

结论

儿童肘部MOT罕见,及时切除病变是获得满意结果的有效治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5f3/12422683/c28a3222b369/JOCR-15-43-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5f3/12422683/e113a9e721f6/JOCR-15-43-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5f3/12422683/8aa4ab39903d/JOCR-15-43-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5f3/12422683/e02336b289b2/JOCR-15-43-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5f3/12422683/d91835b25cec/JOCR-15-43-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5f3/12422683/0fd0af54eb46/JOCR-15-43-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5f3/12422683/80d837953a81/JOCR-15-43-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5f3/12422683/c28a3222b369/JOCR-15-43-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5f3/12422683/e113a9e721f6/JOCR-15-43-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5f3/12422683/8aa4ab39903d/JOCR-15-43-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5f3/12422683/e02336b289b2/JOCR-15-43-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5f3/12422683/d91835b25cec/JOCR-15-43-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5f3/12422683/0fd0af54eb46/JOCR-15-43-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5f3/12422683/80d837953a81/JOCR-15-43-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5f3/12422683/c28a3222b369/JOCR-15-43-g007.jpg

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